Canonical Allele Identifier: CA5921909

Gene: NELL1

Linked Data

• dbSNP Id: rs368949238
• ExAC: 11:20805239 G / T
• gnomAD v2: 11-20805239-G-T
• gnomAD v4: 11-20783693-G-T
• MyVariant Identifiers: chr11:g.20805239G>T (hg19) ; chr11:g.20783693G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20783693G>T , CM000673.2:g.20783693G>T	GRCh38
NC_000011.9:g.20805239G>T , CM000673.1:g.20805239G>T	GRCh37
NC_000011.8:g.20761815G>T	NCBI36
NG_047064.1:g.119143G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357134.10:c.198G>T MANE Select	ENSP00000349654.5:p.Glu66Asp
ENST00000298925.9:c.282G>T	ENSP00000298925.5:p.Glu94Asp
ENST00000325319.9:c.198G>T	ENSP00000317837.5:p.Glu66Asp
ENST00000357134.9:c.198G>T	ENSP00000349654.5:p.Glu66Asp
ENST00000524738.1:n.25G>T
ENST00000527873.5:n.219G>T
ENST00000528046.5:n.381G>T
ENST00000529595.1:n.86G>T
ENST00000532434.5:c.198G>T	ENSP00000437170.1:p.Glu66Asp
ENST00000619031.4:c.-515G>T	ENSP00000479479.1:n.-515G>T
NM_001288713.1:c.282G>T	NP_001275642.1:p.Glu94Asp
NM_001288714.1:c.198G>T	NP_001275643.1:p.Glu66Asp
NM_006157.4:c.198G>T	NP_006148.2:p.Glu66Asp
NM_201551.2:c.198G>T	NP_963845.1:p.Glu66Asp
NM_006157.5:c.198G>T MANE Select	NP_006148.2:p.Glu66Asp